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首页> 外文期刊>Urologic oncology >Genetic polymorphism of glutathione S-transferases M1 and T1 in Egyptian patients with bilharzial bladder cancer.
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Genetic polymorphism of glutathione S-transferases M1 and T1 in Egyptian patients with bilharzial bladder cancer.

机译:埃及比哈兹膀胱癌患者谷胱甘肽S-转移酶M1和T1的遗传多态性。

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OBJECTIVE: To assess the influence of glutathione S-transferases M1 and T1 (GSTM1 and T1) genotype on the risk of bladder cancer in patients with urinary bilharziasis. MATERIALS AND METHODS: This study was designed as a case-control study that involved 60 individuals who were enrolled into 3 equal groups. The first one included patients with bilharzial bladder cancer, the second one had those with nonmalignant urinary bilharziasis, and the last one was the control group. All of the participants were adult males, nonsmokers, and with matched ages. All of them underwent an assessment of the serum level of the total GST concentration and the polymerase chain reaction (PCR) was used for determination of the GSTM1 and T1 genotypes. RESULTS: The lower most GST enzyme concentration was reported in patients with bilharzial bladder cancer (26 +/- 4.4 ng/ml) with significant difference between it and that of the second group (36.8 +/- 4.1 ng/ml, P < 0.05) and that of the controls (40.4 +/- 4 ng/ml, P < 0.005). The PCR results have demonstrated that the frequency of combined GSTM1 and T1 genes deletion (M1-ve T1-ve) was significantly higher in cases of bladder cancer (40%) than those of the controls (5%, P < 0.005) and those of the second group (10%, P < 0.05). The unconditional logistic regression test revealed that patients with urinary bilharziasis and combined GSTM1 and T1 genes deletion are at a significant risk for malignant transformation (OR = 6.3, P < 0.05). CONCLUSIONS: Patients with urinary bilharziasis and GSTM1-ve and T1-ve genes might be at increased risk of bladder cancer. However, larger studies are needed for confirmation of these results.
机译:目的:评估谷胱甘肽S-转移酶M1和T1(GSTM1和T1)基因型对泌尿胆道疾病患者罹患膀胱癌的风险的影响。材料与方法:本研究设计为病例对照研究,涉及60位个体,分为3组。第一个包括胆道膀胱癌患者,第二个包括非恶性尿道胆道疾病患者,最后一个是对照组。所有参与者均为成年男性,不吸烟者,并且年龄匹配。他们都进行了血清总GST浓度的评估,并使用聚合酶链反应(PCR)来确定GSTM1和T1基因型。结果:报告的胆汁性膀胱癌患者的最高GST酶浓度较低(26 +/- 4.4 ng / ml),与第二组相比有显着差异(36.8 +/- 4.1 ng / ml,P <0.05 )和对照(40.4 +/- 4 ng / ml,P <0.005)。 PCR结果表明,膀胱癌病例(40%)中GSTM1和T1基因联合缺失的频率(M1-ve T1-ve)显着高于对照组(5%,P <0.005)和那些第二组(10%,P <0.05)。无条件logistic回归测试显示,患有尿胆原虫病并合并GSTM1和T1基因缺失的患者发生恶性转化的风险很高(OR = 6.3,P <0.05)。结论:患有尿道胆汁淤积和GSTM1-ve和T1-ve基因的患者可能患膀胱癌的风险增加。但是,需要更大的研究来证实这些结果。

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